Skip to main content

Press Releases


Below you will find a list of LEO Pharma's most recent global and affiliate-issued press releases, relevant to LEO Pharma Inc., LEO Pharma’s U.S. business. These press releases are intended for use by media. Please note that you will be linking out to the LEO Pharma global website or the news wire to access these press releases.  

Featured stories 

 

10-26-22 LEO Pharma announces British Journal of Dermatology publication of Adbry™ (tralokinumab-ldrm) pooled safety data in moderate-to-severe atopic dermatitis

 

9-8-22 LEO Pharma presents new Adbry™ (tralokinumab-ldrm) safety data in moderate-to-severe atopic dermatitis at 31st EADV Congress

 

8-25-22 LEO Pharma to present new data in moderate-to-severe atopic dermatitis and chronic hand eczema at the 31st EADV Congress

 

7-20-22 LEO Pharma Announces Publication of Adbry™ (tralokinumab-ldrm) Efficacy Data in Moderate-to-Severe Atopic Dermatitis in American Journal of Clinical Dermatology

 

4-11-22 LEO Pharma Presents New Interim Long-Term Efficacy Data for Adbry™ (tralokinumab-ldrm) in Moderate-to-Severe Atopic Dermatitis at the 2022 RAD Conference

 

3-25-22 LEO Pharma Presents New Interim Long-Term Safety and Efficacy Data for Adbry™ (tralokinumab-ldrm) in Moderate-to-Severe Atopic Dermatitis at the 2022 AAD Annual Meeting

 

2-17-22 LEO Pharma A/S Appoints Brian Hilberdink New President of LEO Pharma Inc. United States

 

12-28-21 LEO Pharma announces FDA approval of Adbry™ (tralokinumab-ldrm) as the first and only treatment specifically targeting IL-13 for adults with moderate-to-severe atopic dermatitis

 

10-22-21 Tralokinumab Achieves Primary and Secondary Endpoints in Phase 3 Trial of Adolescents With Moderate-to-Severe Atopic Dermatitis

 

9-30-21 LEO Pharma presents interim data from Phase 3 tralokinumab long-term extension trial in moderate-to-severe atopic dermatitis at EADV 30th Congress

 

4-29-21 Update on U.S. FDA review of LEO Pharma’s Biologics License Application for tralokinumab for the treatment of adults with moderate-to-severe atopic dermatitis

 

4-23-21 LEO Pharma Presents Long-Term Safety and Efficacy Data for Tralokinumab in Adults With Moderate-to-Severe Atopic Dermatitis at AAD VMX 2021

 

4-23-21 LEO Pharma Receives Positive CHMP Opinion of Adtralza® (tralokinumab) for the Treatment of Adults with Moderate-to-severe Atopic Dermatitis

 

10-29-20 LEO Pharma announces positive results of Phase 2b dose-finding study with delgocitinib cream in adult patients with mild-to-severe chronic hand eczema (CHE)

 

10-29-20 LEO Pharma Presents Data for Tralokinumab on Pooled Safety, S. aureus Colonization Reduction and Impact on Vaccine Response Rates at the 29th Annual European Academy of Dermatology and Venereology (EADV) Virtual Congress

 

10-27-20 LEO Pharma to Highlight New Data in Medical Dermatology at EADV Virtual 2020

 

10-22-20 LEO Pharma Announces U.S. FDA Approval for Enstilar® (calcipotriene and betamethasone dipropionate) Foam U.S. Prescribing Information Update to Include Data in Long-term Use in Plaque Psoriasis Treatment

 

10-16-20 LEO Pharma Announces British Journal of Dermatology Publication of Three Pivotal Ph 3 Trials of Tralokinumab, Demonstrating Safety and Sustained Improvements in Severity and Quality of Life Measures in Adults with Moderate-to-Severe Atopic Dermatitis

 

8-4-20 LEO Pharma announces U.S. Food and Drug Administration Fast Track designation for delgocitinib cream for the treatment of adults with moderate-to-severe chronic hand eczema

MAT-56201 April 2022
Serverside rendering